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rs794728651

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728651(A;C)
Make rs794728651(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807664
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728651
ebirs794728651
HLIrs794728651
Exacrs794728651
Varsomers794728651
Maprs794728651
PheGenIrs794728651
hapmaprs794728651
1000 genomesrs794728651
hgdprs794728651
ensemblrs794728651
gopubmedrs794728651
geneviewrs794728651
scholarrs794728651
googlers794728651
pharmgkbrs794728651
gwascentralrs794728651
openSNPrs794728651
23andMers794728651
23andMe allrs794728651
SNP Nexus

SNPshotrs794728651
SNPdbers794728651
MSV3drs794728651
GWAS Ctlgrs794728651
Max Magnitude0
ClinVar
Risk rs794728651(C;C)
Alt rs794728651(C;C)
Reference rs794728651(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575136T>G
CLNSRC
CLNACC RCV000182451.1,